1+ months

Senior Production Supervisor-Davie, FL.

Davie, FL 33314

Company Info

If youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry.

Tevas Davie and Sunrise (Florida) production sites are two of our largest launch facilities.   We are strengthening and adding to our critical teams with great talent and capabilities. Teva, a global organization, with a brand of evolving success.  Be part of it!


Teva is a global pharmaceutical leader and the worlds largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we have built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

As a Senior Production Supervisor, well count on you to:

Directs and oversees the daily manufacturing process operations. Ensures that all phases of manufacturing activity are performed in a safe manner and in compliance with cGMP and Standard Operating Procedures (SOP's). Ensures that Company and government compliance are adhered to. Critical Success Factors will include maintaining a disciplined Daily Management process utilizing TGO tools (LSW, 5S, Problem Solving, Coaching and Feedback).


  • Supervise and coordinate the manufacturing work schedule to meet production requirements 
  • Assign and delegate work assignment responsibilities to  hourly team members
  • Perform on-going cGMP and safety training to department process operators
  • Ensure safe practices and EHS requirements are carried out, including proper use of PPE, Company equipment, safe handling of materials, and that safety rules and regulations are followed at all times
  • Assure that manufacturing operations are performed in compliance with batch records, SOP's, and cGMP's, and complies with data integrity requirements at all times.
  • Revise batch records and SOP's as required
  • Coordinate with Quality Control Department for timely release of intermediate sample results and packaging final product release
  • Perform full scope supervisory responsibilities including hiring, training, problem resolution, work assignment delegation, performance appraisal and management and attendance tracking
  • Advise Manufacturing Manager of all current manufacturing process issues
  • Improve the efficiency of the operation by analyzing and correcting production equipment and processing problems; troubleshoots equipment by making minor adjustments to compensate for product processing problems with support groups as required 
  • Coordinate with Materials Management, scheduling and quality assurance documentation to ensure scheduling efficiency and batch record audit completion
  • Interface with external contacts/vendors to facilitate the introduction of new equipment.
  • Document non-conformances (completes manufacturing investigations). Gathers data and uses problem solving techniques to determine root cause


  • BA/BS degree with a minimum of 10 years of related production supervisory experience in a regulated, GMP environment
  • Six Sigma Black Belt preferred
  • Demonstrated knowledge of/experience with lean tools Value Stream Mapping, Standard Work, 5S, Kanban & Practical Problem Solving
  • Team leadership and supervisory experience, including complaint/conflict resolution experience
  • Strong working knowledge of Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements
  • Experience analyzing and troubleshooting problems, identifying solutions, recommending and implementing methods, procedures and/or techniques for resolution
  • Oral Solid Dose experience (i.e. Blending, Compression, Encapsulation, Pan Coating, Laser Drill, and Fluid Bed Coating).



Sub Function


Reports To

Sr Mgr Section/API Facility

Tevas Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.


Posted: 2019-06-28 Expires: 2019-08-28

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Senior Production Supervisor-Davie, FL.

Teva Pharmaceuticals
Davie, FL 33314

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast